ENST00000332142.10:c.1715C>T
MANE Select
|
ENSP00000331727.5:p.Ala572Val
|
|
ENST00000328032.8:c.1694C>T
|
ENSP00000333781.4:p.Ala565Val
|
|
ENST00000332142.9:c.1715C>T
|
ENSP00000331727.5:p.Ala572Val
|
|
ENST00000618399.4:c.1415C>T
|
ENSP00000482818.1:p.Ala472Val
|
|
ENST00000621889.1:c.1388C>T
|
ENSP00000483158.1:p.Ala463Val
|
|
NM_033272.3:c.1715C>T
|
NP_150375.2:p.Ala572Val
|
|
NM_173162.2:c.1694C>T
|
NP_775185.1:p.Ala565Val
|
|
XM_011512109.1:c.1739C>T
|
XP_011510411.1:p.Ala580Val
|
|
XM_011512109.3:c.1739C>T
|
XP_011510411.1:p.Ala580Val
|
|
XM_017005218.2:c.1739C>T
|
XP_016860707.1:p.Ala580Val
|
|
XM_017005219.2:c.1715C>T
|
XP_016860708.1:p.Ala572Val
|
|
XM_017005220.2:c.1694C>T
|
XP_016860709.1:p.Ala565Val
|
|
XM_017005221.2:c.1739C>T
|
XP_016860710.1:p.Ala580Val
|
|
NM_033272.4:c.1715C>T
MANE Select
|
NP_150375.2:p.Ala572Val
|
|
NM_173162.3:c.1694C>T
|
NP_775185.1:p.Ala565Val
|
|